货号:A771467
同义名:
5,7-Dihydroxyflavone; 5,7-DHF
Chrysin是一种 apigenin 类似物,能够抑制芳香化酶并调节 PLCY2 和 PKC 的磷酸化活性。可以从蓝色百香果(Passiflora caerulea)中分离,具有抗炎和抗血栓作用等。


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解

| 产品名称 | Aromatase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Exemestane |
+++
Aromatase (human), IC50: 30 nM Aromatase (rat), IC50: 40 nM |
97% | |||||||||||||||||
| Letrozole | 99% | ||||||||||||||||||
| Anastrozole |
+++
Aromatase, IC50: 15 nM |
97% | |||||||||||||||||
| Obacunone |
+
Aromatase, IC50: 28.4 μM |
Nrf2 | 98% | ||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Chrysin, found in passion flowers, honey, and propolis, acts as a potential therapeutic and preventive agent against various human cancers, including ovarian cancer. It inhibits ovarian cancer cell proliferation and induces cell death by increasing ROS production, cytoplasmic Ca2+ levels, and inducing loss of mitochondrial membrane potential. Chrysin activates both MAPK and PI3K/AKT pathways, suppresses tumor growth by regulating Wnt and NF-κB signaling, and stimulates phosphorylation of AKT and P70S6K proteins[1]. |
| 体外研究 | Chrysin, found in passion flowers, honey, and propolis, acts as a potential therapeutic and preventive agent against various human cancers, including ovarian cancer. It inhibits ovarian cancer cell proliferation and induces cell death by increasing ROS production, cytoplasmic Ca2+ levels, and inducing loss of mitochondrial membrane potential. Chrysin activates both MAPK and PI3K/AKT pathways, suppresses tumor growth by regulating Wnt and NF-κB signaling, and stimulates phosphorylation of AKT and P70S6K proteins[1]. |
| Concentration | Treated Time | Description | References | |
| Mouse embryonic fibroblasts | 25 µM | 24 hours | Investigate the effect of xanthosine on cellular metabolome, results showed xanthosine downregulated metabolites involved in cholesterol and uric acid synthesis pathways | Int J Mol Sci. 2023 Feb 17;24(4):4066 |
| SW620 cells | 10 and 20 μM | 48 hours | Chrysin inhibits EMT and malignant progression of colorectal cancer cells by inhibiting the COMP/TAGLN complex. | Theranostics. 2020 Jul 9;10(19):8790-8806. |
| HCT-8 cells | 10 and 20 μM | 48 hours | Chrysin inhibits EMT and malignant progression of colorectal cancer cells by inhibiting the COMP/TAGLN complex. | Theranostics. 2020 Jul 9;10(19):8790-8806. |
| HCT116 cells | 10 and 20 μM | 48 hours | Chrysin inhibits EMT and malignant progression of colorectal cancer cells by inhibiting the COMP/TAGLN complex. | Theranostics. 2020 Jul 9;10(19):8790-8806. |
| SK-BR-3 cells | 20 μM | Induce cell cycle arrest and inhibit proliferation | Signal Transduct Target Ther. 2023 Dec 18;8(1):463. | |
| BT-474 cells | 20 μM | Inhibit proliferation of HER2-positive breast cancer cells | Signal Transduct Target Ther. 2023 Dec 18;8(1):463. | |
| MC3T3-E1 cells | 25 μmol/L | 15 min | Activated ERK1/2 phosphorylation, promoted osteogenic differentiation | Protein Cell. 2013 Jul;4(7):539-47. |
| MC3T3-E1 cells | 25 μmol/L | 96 h | Upregulated Runx2 and Osx gene expression, promoted osteogenic differentiation | Protein Cell. 2013 Jul;4(7):539-47. |
| MC3T3-E1 cells | 25 μmol/L | 14 d | Promoted osteogenic differentiation, significantly enhanced mineralization nodule formation | Protein Cell. 2013 Jul;4(7):539-47. |
| MC3T3-E1 cells | 0–100 μmol/L | 72 h and 96 h | Assessed cytotoxicity, results showed no cytotoxicity at concentrations below 50 μmol/L | Protein Cell. 2013 Jul;4(7):539-47. |
| Bel-7402 | 30μM | 8h | Inhibited glycolysis and induced apoptosis | J Exp Clin Cancer Res. 2017 Mar 20;36(1):44. |
| SMMC-7721 | 30μM | 8h | Inhibited glycolysis and induced apoptosis | J Exp Clin Cancer Res. 2017 Mar 20;36(1):44. |
| HCC-LM3 | 30μM | 8h | Inhibited glycolysis and induced apoptosis | J Exp Clin Cancer Res. 2017 Mar 20;36(1):44. |
| RAW264.7 monocyte/macrophages | 50μM | 6 hours | To investigate the inhibitory effect of Chrysin on LPS and IFNγ-induced iNOS gene expression. Results showed that Chrysin significantly attenuated the expression of iNOS gene. | Br J Pharmacol. 1996 Aug;118(8):2178-84. |
| HepG2 cells | 1 or 10 µM | 24 hours | Assess AhR agonist activity, Chrysin activated gene expression in HepG2 cells | Environ Health Perspect. 2003 Dec;111(16):1877-82. |
| MCF-7 cells | 1 or 10 µM | 24 hours | Assess AhR agonist activity, 10 µM Chrysin induced a 5.5-fold increase in luciferase activity | Environ Health Perspect. 2003 Dec;111(16):1877-82. |
| Hepa-1 cells | 1 or 10 µM | 24 hours | Assess AhR agonist activity, 10 µM Chrysin induced a 14-fold increase in luciferase activity | Environ Health Perspect. 2003 Dec;111(16):1877-82. |
| IPSCs-derived neurons | 100 μM | 20 minutes | Evaluate the inhibitory effect of Chrysin on spontaneous discharges and 4-AP-induced epileptiform activity. Results showed that Chrysin significantly inhibited spontaneous discharges at 100 μM but had no significant effect on 4-AP-induced epileptiform activity. | J Adv Res. 2024 Oct;64:249-262. |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | Experimental autoimmune uveitis (EAU) | Intragastric | 25 mg/kg | Once daily from 3 days before immunization to 21 days after immunization | Chrysin significantly reduced the clinical and histopathological scores of EAU, increased the integrity of the blood-retinal barrier, and enhanced the expression of tight junction proteins. Additionally, Chrysin significantly decreased the proportions of Th1, Th17, and CD4+CD3+CD62L+Th0 cells while increasing the proportion of Treg cells. Chrysin also inhibited macrophage infiltration and the expression of inducible nitric oxide synthase in the retina, reduced the expression of interferon-γ, IL-17A, IL-6, IL-1β, and tumor necrosis factor-α, and elevated the levels of transforming growth factor-β. Furthermore, NF-κBp65 expression was downregulated after Chrysin treatment. | Cell Mol Immunol. 2017 Aug;14(8):702-711 |
| BALB/c nude mice | Subcutaneous xenograft model of colorectal cancer | Intraperitoneal injection | 20 mg/kg | Once daily until the endpoint of the experiment | Chrysin significantly inhibited the growth and metastasis of colorectal cancer. | Theranostics. 2020 Jul 9;10(19):8790-8806. |
| BALB/c nude mice | HER2-positive breast cancer xenograft model | Gavage | 50 mg/kg | Once daily for 21 days | Inhibit tumor growth | Signal Transduct Target Ther. 2023 Dec 18;8(1):463. |
| Nude mice | HCC-LM3 xenograft model | Intraperitoneal injection | 30 mg/kg | Three times weekly | Inhibited tumor growth and decreased HK-2 expression | J Exp Clin Cancer Res. 2017 Mar 20;36(1):44. |
| Zebrafish | PTZ-induced seizure model | Incubation | 100 μg/mL | 20 minutes | Evaluate the inhibitory effect of Chrysin on PTZ-induced seizure activity. Results showed that Chrysin had no significant anti-seizure effect at 100 μg/mL. | J Adv Res. 2024 Oct;64:249-262. |
| Dose | Mice: 0.6 mg/kg - 10 mg/kg[6] (i.p.), 50 mg/kg[7] (I.p.) Rat: 25 mg/kg - 100 mg/kg[8] (p.o.), 3 mg/kg - 30 mg/kg[9] (p.o.) |
| Administration | i.p., p.o. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.93mL 0.79mL 0.39mL |
19.67mL 3.93mL 1.97mL |
39.33mL 7.87mL 3.93mL |
|
| CAS号 | 480-40-0 |
| 分子式 | C15H10O4 |
| 分子量 | 254.24 |
| SMILES Code | O=C1C=C(C2=CC=CC=C2)OC3=CC(O)=CC(O)=C13 |
| MDL No. | MFCD00006834 |
| 别名 | 5,7-Dihydroxyflavone; 5,7-DHF; Galangin flavanone.; NP005901; NSC 407436 |
| 运输 | 蓝冰 |
| InChI Key | RTIXKCRFFJGDFG-UHFFFAOYSA-N |
| Pubchem ID | 5281607 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry,2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(413 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
|
沪公网安备 31011702889066号
沪ICP备2024050318号-1